ClinVar Miner

List of variants in gene ARHGEF9 reported as benign for X-linked syndromic intellectual disability

Included ClinVar conditions (212):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 3
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HGVS dbSNP
NM_001353921.2(ARHGEF9):c.29T>C (p.Met10Thr) rs1421919089
NM_001353921.2(ARHGEF9):c.675G>A (p.Gln225=) rs140777637
NM_001353921.2(ARHGEF9):c.939C>G (p.Asp313Glu) rs143490560

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